Methanol → 4-Bromo-2-fluoro-1-(methylsulfonyl)benzene

HRID 732747Notes

Reaction equation

HRID 732747 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](SC)=[C:4]([F:10])[CH:3]=1.O[O:12][S:13]([O-:15])=O.[K+].[CH3:17]O>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:13]([CH3:17])(=[O:15])=[O:12])=[C:4]([F:10])[CH:3]=1

Participants

4

Procedure

Combine 4-bromo-2-fluorothioanisole (U.S. Pat. No. 6,307,047, 2.7 g, 12 mmol), oxone (38 g, 62 mmol) and methanol (200 mL) and stir for 12 hours. Filter through a pad of silica gel and elute with ethyl acetate (500 mL). Evaporate solvent and partition between dichloromethane (200 mL) and water (100 mL). Separate the layers, wash the organic layer with saturated aqueous NaHCO3 (10 mL), brine (10 mL), dry with MgSO4, filter, and concentrate in vacuo. Wash the crude solid with hexane (20 mL), ether (10 mL) and dry in vacuo to obtain 2.4 g of 4-bromo-2-fluoro-1-methanesulfonyl-benzene 78%).

Workup

  1. filtrationFilter through a pad of silica gel
  2. washelute with ethyl acetate (500 mL)
  3. customEvaporate solvent and partition between dichloromethane (200 mL) and water (100 mL)
  4. customSeparate the layers
  5. washwash the organic layer with saturated aqueous NaHCO3 (10 mL), brine (10 mL)
  6. dry with materialdry with MgSO4
  7. filtrationfilter
  8. concentrationconcentrate in vacuo
  9. washWash the crude solid with hexane (20 mL), ether (10 mL)
  10. customdry in vacuo

Sources & evidence

ORD record
ord-df245f42fad2451ea51e0b3aadfd4f82
Source dataset
uspto-grants-2009_09
Patent number
US07585977B2

Reaction notes

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